首页|桂郁金醇提物对脂多糖致小鼠肺损伤的保护作用研究

桂郁金醇提物对脂多糖致小鼠肺损伤的保护作用研究

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[目的]研究桂郁金醇提物对脂多糖(LPS)致小鼠急性肺损伤(ALI)的保护作用。[方法]将54只雄性昆明小鼠随机分成6组:空白组、模型组、地塞米松阳性对照组及桂郁金醇提物低(2 g/kg)、中(4 g/kg)、高(40 g/kg)剂量组,每组9只。给药组小鼠分别灌胃给予地塞米松(5 mg/kg)或相应浓度桂郁金醇提物混悬液(0。2 mL/10 g),空白组和模型组小鼠灌胃给予相应体积的0。5%羧甲基维生素钠(CMC-Na),连续灌胃5 d。末次给药1 h后,除空白组外,其余各组小鼠腹腔注射10 mg/kg LPS,12 h后麻醉并处死小鼠,剖取肺脏组织。试验中观察造模前后小鼠一般情况变化,统计小鼠体重变化、肺脏指数,测定肺脏重湿/干比。通过HE染色观察小鼠肺脏组织病理学变化并进行肺损伤评分;利用实时荧光定量PCR检测肺脏组织中炎症因子肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、髓样分化因子88(MyD88)、Toll样受体4(TLR4)、核转录因子KB(NF-KB)mRNA表达水平。[结果]与空白组相比,模型组小鼠体重增长率极显著下降(P<0。01),肺脏指数、肺脏重湿/干比和肺损伤总评分均极显著升高(P<0。01),肺脏组织相关炎症因子mRNA相对表达量均显著或极显著增加(P<0。05;P<0。01),成功构建ALI小鼠模型。与模型组相比,桂郁金醇提物各剂量组小鼠体重增长率显著或极显著升高(P<0。05;P<0。01);桂郁金醇提物中、高剂量组小鼠肺脏指数、肺脏重湿/干比均显著或极显著降低(P<0。05;P<0。01);桂郁金醇提物高剂量组小鼠肺损伤总评分和肺脏组织中TNF-α、IL-6基因mRNA表达量显著降低(P<0。05);桂郁金醇提物中剂量组小鼠肺脏组织中NF-κB基因mRNA表达量显著降低(P<0。05)。[结论]桂郁金醇提物对LPS诱导的小鼠ALI具有保护作用,其作用机制可能与桂郁金醇提物减轻TLR4/MyD88/NF-κB信号通路介导的炎症损伤有关。
Protective Effect of Alcohol Extract from Curcuma kwangsiensis on Lung Injury Induced by LPS in Mice
[Objective]The objective of this study was to investigate the protective effect of alcohol extract from Curcuma kwangsiensis on acute lung injury(ALI)induced by lipopolysaccharide(LPS)in mice.[Method]A total of 54 male Kunming mice were randomly divided into 6 groups:Blank,model,dexamethasone positive control,and alcohol extract from Curcuma kwangsiensis low(2 g/kg),medium(4 g/kg)and high(40 g/kg)groups,with 9 mice in each group.Administration groups were given dexamethasone(5 mg/kg)or corresponding concentration of alcohol extract from Curcuma kwangsiensis(0.2 mL/10 g)by intragastric administration,respectively.Mice in blank and model groups were given the corresponding volume of 0.5%carboxymethyl sodium vitamin(CMC-Na)by intragastric administration for 5 days.1 h after the last administration,except for blank group,mice in other groups were intraperitoneally injected with 10 mg/kg LPS,anesthetized and killed 12 h later,and lung tissue was dissected.During the experiment,the general conditions of mice before and after modeling were observed,the changes of body weight and lung index of mice were counted,and the ratio of wet weight to dry weight of lung was measured.HE staining was used to observe the lung histopathological changes and lung injury score.Real-time quantitative PCR was used to detect the mRNA expression of inflammatory factors,including tumor necrosis factor-alpha(TNF-α),interleukin-6(IL-6),myeloid differentiation factor 88(MyD88),Toll-like receptor 4(TLR4)and nuclear transcription factor κB(NF-κB)in lung.[Result]Compared with blank group,the body weight growth rate of mice in model group was extremely significantly decreased(P<0.01),the lung index,the ratio of wet weight to dry weight of lung and total lung injury score were extremely significantly increased(P<0.01),and the mRNA relative expression of related inflammatory factors was significantly or extremely significantly increased(P<0.05 or P<0.01),the ALI model was suscessfully constructed.Compared with model group,the body weight growth rate of mice in each dose group of alcohol extract from Curcuma kwangsiensis was significantly or extremely significantly increased(P<0.05 or P<0.01).The lung index and the ratio of wet weight to dry weight of lung in medium and high dose groups of alcohol extract from Curcuma kwangsiensis were significantly or extremely significantly decreased(P<0.05 or P<0.01).The total lung injury score and the mRNA expression of TNF-α and IL-6 genes in lung of mice in high dose group of alcohol extract from Curcuma kwangsiensis were significantly decreased(P<0.05).The mRNA expression of NF-κB gene in lung of mice in medium dose group of alcohol extract from Curcuma kwangsiensis was significantly decreased(P<0.05).[Conclusion]Alcohol extract from Curcuma kwangsiensis had a protective effect on LPS-induced ALI in mice,and its mechanism might be related to the reduction of inflammatory damage mediated by TLR4/MyD88/NF-κB signaling pathway.

alcohol extract from Curcuma kwangsiensislipopolysaccharidemiceacute lung injuryTLR4/MyD88/NF-κB pathway

胡明霞、邓艳萍、何永芸、姚玥、莫晓丹、黄安、杨秀芬

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广西中医药大学药学院,广西壮瑶药重点实验室,广西高校中药神经-代谢及免疫药理重点实验室,南宁 530200

桂郁金醇提物 脂多糖 小鼠 急性肺损伤 TLR4/MyD88/NF-κB通路

广西自然科学基金广西壮瑶药重点实验室建设项目计划基金广西壮瑶药重点实验室建设项目计划基金中药学广西一流学科建设项目

2020GXNSFAA297165GXZYZZ2022-08GXZYYZZ2023-03桂教科研[2022]1号

2024

中国畜牧兽医
中国农业科学院北京畜牧兽医研究所

中国畜牧兽医

CSTPCD北大核心
影响因子:0.72
ISSN:1671-7236
年,卷(期):2024.51(8)